{"database":"GEO","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Other":["ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE296nnn/GSE296489/"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"omics_type":["Genomics"],"species":["Homo sapiens"],"gds_type":[" SNP genotyping by SNP array","Genome variation profiling by SNP array"],"full_dataset_link":["https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE296489"],"repository":["GEO"],"entry_type":["GSE"],"additional_accession":[]},"is_claimable":false,"name":"Clinical Phenotype and Genetic Analysis of a Family with 17q12 Microdeletion Syndrome","description":"To clarify the genetic etiology of a 17q12 microdeletion syndrome fetus in a family and analyze the correlation between the genetic and clinical phenotypes within the family. The child and her father, who share the same genetic variation, exhibit significant clinical heterogeneity.","dates":{"publication":"2026/05/07"},"accession":"GSE296489","cross_references":{"GSM":["GSM8971576","GSM8971577","GSM8971578","GSM8971579"],"GPL":["18637"],"GSE":["296489"],"taxon":["Homo sapiens"]}}